Therapeutic Potential of Inulin‐Coated MCT Microcapsules in Modulating the Gut Microbiome for Effective Treatment of Diet‐Induced Obesity

Author:

Ariaee Amin1,Wardill Hannah R.2,Wignall Anthony1,Elz Aurelia S.13,Wright Leah4,Prestidge Clive1,Joyce Paul1ORCID

Affiliation:

1. UniSA Clinical and Health Sciences University of South Australia Adelaide South Australia 5000 Australia

2. Translational Oncology Laboratory Centre for Cancer Biology University of South Australia and SA Pathology Adelaide South Australia 5000 Australia

3. School of Biomedicine The University of Adelaide Adelaide 5000 Australia

4. School of Chemical Engineering The University of Adelaide Adelaide 5000 Australia

Abstract

AbstractObesity, a global epidemic, leads to metabolic dysregulation and systemic inflammation. Recently, therapies targeting the gut microbiome have garnered attention for metabolic health regulation. This study evaluates the potential of inulin‐coated medium‐chain triglyceride (InuMCT) microcapsules in rats with diet‐induced obesity (DIO). Inulin prebiotic fibers have been shown to promote the gut microbiome, while the digestion products of medium chain triglycerides (MCTs), free fatty acids, and mono‐/diglycerides, can attenuate pro‐inflammatory outcomes. It is hypothesized that encapsulating MCTs within inulin via spray drying creates a solid dosage form that can exert multifunctional effects in ameliorating inflammation in DIO. Inulin and InuMCT treatments not only reduce DIO weight gain but also improve metabolic markers in high‐fat diet (HFD) fed rats. Specifically, inulin attenuates the reduction of high‐density lipoprotein (HDL) by 55% and lowers glucose levels by 21%. Meanwhile, InuMCT increases HDL by 23% and reduces glucose levels by 15%. Furthermore, inulin decreases serum proinflammatory tumor necrosis factor‐alpha (TNF‐α) by 35%, while InuMCT further reduces TNF‐α to normal diet levels within 21 days. These results highlight InuMCT's superior efficacy, offering a promising strategy for combating obesity and related metabolic diseases.

Funder

Hospital Research Foundation

Publisher

Wiley

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